1. Academic Validation
  2. Discovery of a novel class of dimeric Smac mimetics as potent IAP antagonists resulting in a clinical candidate for the treatment of cancer (AZD5582)

Discovery of a novel class of dimeric Smac mimetics as potent IAP antagonists resulting in a clinical candidate for the treatment of cancer (AZD5582)

  • J Med Chem. 2013 Dec 27;56(24):9897-919. doi: 10.1021/jm401075x.
Edward J Hennessy 1 Ammar Adam Brian M Aquila Lillian M Castriotta Donald Cook Maureen Hattersley Alexander W Hird Christopher Huntington Victor M Kamhi Naomi M Laing Danyang Li Terry MacIntyre Charles A Omer Vibha Oza Troy Patterson Galina Repik Michael T Rooney Jamal C Saeh Li Sha Melissa M Vasbinder Haiyun Wang David Whitston
Affiliations

Affiliation

  • 1 Oncology iMed, Innovative Medicines & Early Development, AstraZeneca R&D Boston , 35 Gatehouse Drive, Waltham, Massachusetts 02451, United States.
Abstract

A series of dimeric compounds based on the AVPI motif of Smac were designed and prepared as antagonists of the inhibitor of Apoptosis proteins (IAPs). Optimization of cellular potency, physical properties, and pharmacokinetic parameters led to the identification of compound 14 (AZD5582), which binds potently to the BIR3 domains of cIAP1, cIAP2, and XIAP (IC50 = 15, 21, and 15 nM, respectively). This compound causes cIAP1 degradation and induces Apoptosis in the MDA-MB-231 breast Cancer cell line at subnanomolar concentrations in vitro. When administered intravenously to MDA-MB-231 xenograft-bearing mice, 14 results in cIAP1 degradation and Caspase-3 cleavage within tumor cells and causes substantial tumor regressions following two weekly doses of 3.0 mg/kg. Antiproliferative effects are observed with 14 in only a small subset of the over 200 Cancer cell lines examined, consistent with other published IAP inhibitors. As a result of its in vitro and in vivo profile, 14 was nominated as a candidate for clinical development.

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